ClearanceBrief
510(k) K813487 ยท FKX System, Peritoneal, Automatic Delivery

CATHETER BUBBLE STAND

ApplicantAccurate Surgical Instruments Co., Walker MI, US
DecisionSubstantially Equivalent, Dec 31, 1981
ReceivedDec 1, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K813487

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.